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Rapid Desensitization for Immediate Hypersensitivity to Galsulfase Therapy in Patients with MPS VI

Tamay, Zeynep; Gokcay, Gulden; Dilek, Fatih; Balci, Mehmet Cihan; Ozceker, Deniz; Demirkol, Mubeccel; Guler, Nermin (SPRINGER-VERLAG BERLIN, 2016)

Mucopolysaccharidosis type VI (MPS VI) is a progressive, chronic, and multisystem lysosomal storage disease. Enzyme replacement therapy (ERT) with the recombinant human arylsulfatase B enzyme (galsulfase [Naglazyme]) is ...